607-60-3

Basic information

• Product Name: NAPHTHALEN-1-YL-PROPYLAMINE
• Synonyms: NAPHTHALEN-1-YL-PROPYLAMINE
• CAS NO: 607-60-3
• Molecular Formula: C13H15N
• Molecular Weight: 185.26
• Mol File: 607-60-3.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 322.4°Cat760mmHg
• Flash Point: 157.1°C
• Appearance: /
• Density: 1.052g/cm³
• Vapor Pressure: 0.000279mmHg at 25°C
• Refractive Index: 1.634
• CAS DataBase Reference: NAPHTHALEN-1-YL-PROPYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: NAPHTHALEN-1-YL-PROPYLAMINE(607-60-3)
• EPA Substance Registry System: NAPHTHALEN-1-YL-PROPYLAMINE(607-60-3)

Safety Data

• Hazardous Substances Data: 607-60-3(Hazardous Substances Data)

Usage

General Description

Naphthalen-1-yl-propylamine, also known as 1-Naphthylpropylamine, is an organic chemical compound with the molecular formula C13H13N. It is classified as an aromatic amine and has a strong, distinctive odor. This chemical is primarily used in the production of pharmaceuticals, specifically as a precursor in the synthesis of various drugs and medication. It is also used in the manufacturing of pesticides and dyes. Naphthalen-1-yl-propylamine is considered to be a hazardous substance and should be handled with caution due to its potential health and environmental risks.

InChI:InChI=1/C13H15N/c1-2-10-14-13-9-5-7-11-6-3-4-8-12(11)13/h3-9,14H,2,10H2,1H3

Upstream product

• 107-10-8 propylamine 
• 90-14-2 1-Iodonaphthalene 
• 134-32-7 1-amino-naphthalene 
• 106-94-5 propyl bromide 
• 22950-23-8 N-(2-propenyl)-1-naphthylamine 
• 201230-82-2 carbon monoxide 

Relevant articles and documents

Novel long alkyl side chain benzo[a]phenoxazinium chlorides: synthesis, photophysical behaviour and DNA interaction

Several fluorescent benzo[a]phenoxazinium chlorides possessing a propyl-, octyl-, decyl-, dodecyl- or tetradecylamino at the 5-position of the heterocyclic moiety were efficiently synthesised. The absorption and emission maxima of all compounds lie in the

BENZOPHENOXAZINE DERIVATIVES FOR DIAGNOSIS OF NEOPLASIA OR INFECTION

The present disclosure is related to the synthesis and applications of a benzo[a]phenoxazine. It displays good photophysical properties, such as high molar extinction coefficient, good fluorescence quantum yield and solubility in water. The present invent

N-(di)icosyl-substituted benzo[a]phenoxazinium chlorides: Synthesis and evaluation as near-infrared membrane probes

Five benzo[a]phenoxazinium chlorides containing alkyl chains with twenty carbon atoms at the 5- or 9-positions of the tetracyclic ring were efficiently synthesised and characterised by UV/Vis and NIR spectroscopy. The absorption and emission maxima in ethanol occur in the range 627-641 nm and 645-676 nm, respectively, with quantum yields varying from 0.14 to 0.38. Preliminary photophysical studies with these fluorochromophores in zwitterionic [2,3-bis(palmitoyloxy)propyl-2-(trimethylammonio)ethyl phosphate, DPPC] and cationic (N,N-dimethyl-N-octadecyloctadecan-1-aminium bromide, DODAB) vesicles were carried out. The results showed that the new benzo[a]phenoxazinium derivatives are able to detect the gel to liquid-crystalline lipid phase transition through variations in either the extent of H-aggregation or in the acid-base equilibrium. Novel benzo[a]phenoxazinium chlorides possessing icosyl groups as substituents at the 5- or 9-positions of the tetracyclic ring were photophysically studied in both zwitterionic and cationic vesicles. The results revealed that these fluorochromophores are able to detect the gel to liquid-crystalline lipid phase transition through variations either in the extent of H-aggregation or in an acid-base equilibrium. Copyright